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Clinical Trial Details — Status: Suspended

Administrative data

NCT number NCT01218490
Other study ID # SC 07/12-H
Secondary ID
Status Suspended
Phase Phase 3
First received
Last updated
Start date December 9, 2008
Est. completion date May 2026

Study information

Verified date May 2019
Source Institut Cancerologie de l'Ouest
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

It is a multicenter randomized trial of superior cleaning compared the absence of dissection in stage III patients with optimal surgical resection without retroperitoneal lymph node palpable.


Recruitment information / eligibility

Status Suspended
Enrollment 450
Est. completion date May 2026
Est. primary completion date May 2026
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Age> 18 years

- Karnofsky> 80, or ASA I-II

- Primary ovarian adenocarcinoma, or primitive peritoneal

- No retroperitoneal lymph node> 2cm (CT; MRI)

- Complete surgical staging

- Stage III-IV FIGO classification

- Indication of systemic chemotherapy before surgery or post surgery

Exclusion Criteria:

- Non Invasive Cancer

- non-epithelial or borderline cancer

- Pregnancy

- Previous pelvic lymphadenectomy or aortic-cava for a disease other than ovarian cancer

- Contraindication to Platinum and Paclitaxel

- Borderline Ovarian Tumor

- tumor recurrence

- Incomplete surgery, resectable lesion, Surgery sub optimal (R> 1cm)

Study Design


Intervention

Procedure:
ovarian cancer surgery


Locations

Country Name City State
France Clinique Sainte Thérèse Amiens
France Centre Paul Papin Angers
France Hospital Angers
France Hospital Brest
France Centre Jean Perrin Clermont-Ferrand
France Centre G F Leclerc Dijon
France Hospital Lyon
France Institut Paoli Calmette Marseille
France Centre Val d'Aurelle Montpellier
France Hôpital des Diaconesses Paris
France Hôpital Européen Georges Pompidou Paris
France Hôpital Lariboisière Paris
France Clinique Mutualiste Rennes
France Hopital Rennes
France Centre René Huguenin Saint Cloud
France Institut Cancerologie de l'Ouest Saint Herblain
France Centre Paul Strauss Strasbourg
France Institut Claudius Regaud Toulouse
France Hôpital Bretonneau Tours

Sponsors (1)

Lead Sponsor Collaborator
Institut Cancerologie de l'Ouest

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary survival with out recurrence 5 years
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